Zobrazeno 1 - 10
of 62
pro vyhledávání: '"Mitsumasa, Fukuda"'
Autor:
Yumie Tamura, Mitsumasa Fukuda, Akihiko Ishiyama, Hiroya Nishida, Hirofumi Kashii, Hideaki Mashimo, Kenji Inoue, Hiroshi Sakuma, Satoko Kumada
Publikováno v:
Epilepsy & Behavior Reports, Vol 27, Iss , Pp 100704- (2024)
Anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis in children often requires early immunosuppressive therapy before antibody detection. While various electroencephalogram (EEG) patterns, including extreme delta brushes (EDBs), have been reporte
Externí odkaz:
https://doaj.org/article/e1c769e8e9404849885cdeaca4641b2c
Autor:
Atsuko Arisaka, Mitsuko Nakashima, Satoko Kumada, Kenji Inoue, Hiroya Nishida, Hideaki Mashimo, Hirofumi Kashii, Mitsuhiro Kato, Koichi Maruyama, Akihisa Okumura, Hirotomo Saitsu, Naomichi Matsumoto, Mitsumasa Fukuda
Publikováno v:
Epilepsy & Behavior Reports, Vol 15, Iss , Pp 100417- (2021)
Epileptic-dyskinetic encephalopathies are rare epilepsies characterized by early-onset epileptic encephalopathies (EOEEs) with involuntary movement. Herein, we investigated the impact of gene variants in epileptic-dyskinetic encephalopathies. Four in
Externí odkaz:
https://doaj.org/article/5aa5f75829aa4b3ab1081303d2ac18bb
Autor:
Kenko, Azuma, Shiro, Horisawa, Hideaki, Mashimo, Mitsumasa, Fukuda, Satoko, Kumada, Takakazu, Kawamata, Takaomi, Taira, Hiroyuki, Akagawa
Publikováno v:
Clinical Genetics. 103:209-213
SGCE myoclonus-dystonia is a monogenic form of dystonia with an autosomal dominant mode of inheritance that co-occurs with a myoclonic jerk. In this study, we present 12 Japanese patients from nine families with this disease. Targeted next-generation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::485274b53876801174611be0a5e5c473
https://doi.org/10.1111/cge.14233
https://doi.org/10.1111/cge.14233
Autor:
Manami Mizumoto, Fumihiro Ochi, Toshihiro Jogamoto, Kentaro Okamoto, Mitsumasa Fukuda, Toshifumi Yamauchi, Toyohisa Miyata, Ryo Tashiro, Mariko Eguchi, Riko Kitazawa, Eiichi Ishii
Publikováno v:
Case Reports in Pediatrics, Vol 2019 (2019)
Background. Nonocclusive mesenteric ischemia (NOMI) defines acute mesenteric ischemia without occlusion of the mesenteric arteries. The most common cause of NOMI is vasoconstriction or vasospasm of a mesenteric artery. NOMI generally affects patients
Externí odkaz:
https://doaj.org/article/b51266a35db64db0be0d7d0de1671367
Autor:
Mitsumasa Fukuda, Maya Tojima, Kenji Inoue, Hideaki Mashimo, Hirofumi Kashii, Satoko Kumada, Kiyohide Usami, Akio Ikeda
Publikováno v:
Epileptic Disorders.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9dc3a0413f29cacb5b49e5c4117f36e0
https://doi.org/10.1002/epd2.20047
https://doi.org/10.1002/epd2.20047
Autor:
Satoko Kumada, Kenji Inoue, Takashi Komori, Hideaki Mashimo, Keisuke Takai, Harushi Mori, Mitsumasa Fukuda, Hiromi Suzuki, Hiroya Nishida, Michiharu Morino, Yasuhiro Nakata, Atsuko Arisaka
Publikováno v:
Brain and Development. 42:675-679
Aggressive immunosuppressive therapies have been proposed to treat primary angiitis of the central nervous system (PACNS). Here, we report the first successfully stabilized case of childhood, small-vessel PACNS with intravenous immunoglobulin (IVIG)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e270a5e92b85a55a3869f0d22064f56f
https://doi.org/10.1016/j.braindev.2020.06.007
https://doi.org/10.1016/j.braindev.2020.06.007
Autor:
Mitsumasa Fukuda, Kentaro Okamoto
Publikováno v:
Epilepsy & Seizure. 12:8-13
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b04fc97977fca93800766e84d278c206
https://doi.org/10.3805/eands.12.8
https://doi.org/10.3805/eands.12.8
Publikováno v:
PLoS ONE, Vol 7, Iss 8, p e42920 (2012)
Febrile seizures (FS) is the most common convulsive disorder in children, but there have been no clinical and experimental studies of the possible treatment of FS with herbal medicines, which are widely used in Asian countries. Paeoniflorin (PF) is a
Externí odkaz:
https://doaj.org/article/375170bc5b2547c3b361ccfb7d9af529
Publikováno v:
Brain and Development. 40:904-908
Introduction Epilepsy is a common childhood neurological condition and a major public health concern worldwide. A higher incidence of epilepsy is reported in low- and middle-income countries, particularly in rural areas. However, no Japanese reports
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2fe1122911d282d9f66d952632b73e5a
https://doi.org/10.1016/j.braindev.2018.06.003
https://doi.org/10.1016/j.braindev.2018.06.003
Publikováno v:
Brain and Development. 39:613-616
Many studies have evaluated surgical treatments for spinal deformities in patients with neuromuscular disease. However, few reports have described patients with Fukuyama congenital muscular dystrophy (FCMD). A 13-year-old boy with FCMD was unable to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1fd803928c65ac529a64ca5f5631d7b1
https://doi.org/10.1016/j.braindev.2017.02.003
https://doi.org/10.1016/j.braindev.2017.02.003